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Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease

Abstract

Behçet's disease is an inflammatory disease characterized by recurrent oral and genital ulcers and significant organ involvement. Localizing the genetic association between HLA-B*51 and Behçet's disease and exploring additional susceptibility loci in the human leukocyte antigen (HLA) region are complicated by the strong linkage disequilibrium in this region. We genotyped 8,572 variants in the extended HLA locus and carried out imputation and meta-analysis of 24,834 variants in 2 independent Behçet's disease cohorts from 2 ancestry groups. Genotyped SNPs were used to infer classical HLA alleles in the HLA-A, HLA-B, HLA-C, HLA-DQA1, HLA-DQB1 and HLA-DRB1 loci. Our data suggest that the robust HLA-B*51 association in Behçet's disease is explained by a variant located between the HLA-B and MICA genes (rs116799036: odds ratio (OR) = 3.88, P = 9.42 × 10−50). Three additional independent genetic associations within PSORS1C1 (rs12525170: OR = 3.01, P = 3.01 × 10−26), upstream of HLA-F-AS1 (rs114854070: OR = 1.95, P = 7.84 × 10−14) and with HLA-Cw*1602 (OR = 5.38, P = 6.07 × 10−18) were also identified and replicated.

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Figure 1: Genetic association in the HLA region in individuals with Behçet's disease.
Figure 2: Meta-analysis results of 24,834 markers genotyped or imputed in the HLA region in both the Turkish and Italian cohorts included in this study.

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Acknowledgements

Funding for this project was provided by the Rheumatology Research Foundation's Rheumatology Investigator award to A.H.S. Genotyping of the Italian controls has been made possible by grants from the Celiac Disease Consortium (an innovative cluster approved by the Netherlands Genomics Initiative and partly funded by the Dutch government, grant BSIK03009 to C.W.) and the Netherlands Organization for Scientific Research (NWO-VICI grant 918.66.620 to C.W.).

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Contributions

T.H. performed data analysis and contributed to data interpretation and to the writing of the manuscript. P.C. contributed to performing the experiments and to data analysis. A.A. performed genotyping experiments. V.Y., K.A., N.D., G.K., A.C., A.Y., A.E., E.A., C.S., B.C. and I.K. provided samples for the study. J.G.-A. and C.W. provided genotyping data from Italian controls for the study. H.D. and G.S.-D. provided samples and contributed to the organization of the study. A.H.S. designed and conceived the study, directed the analysis, interpreted the data and wrote the manuscript. All authors contributed to critically reviewing the manuscript.

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Correspondence to Amr H Sawalha.

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The authors declare no competing financial interests.

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Supplementary Figures 1–3 and Supplementary Tables 1–24 (PDF 1811 kb)

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Hughes, T., Coit, P., Adler, A. et al. Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease. Nat Genet 45, 319–324 (2013). https://doi.org/10.1038/ng.2551

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